Long-term monitoring of polarization-mode dispersion of aerial optical cables with respect to line availability von Nellen, P.M., Bronnimann, R., Held, M., Sennhauser, U.

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Darier disease: discrete phenotype in a Sinhalese patient with Darier disease von Nellen, R.G.L., Arits, A.H.M.M., van Geel, M., Steijlen, P.M., van Steensel, M.A.M.

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Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene: Correspondence von Nellen, R.G.L., Steijlen, P.M., Hennies, H.C., Fischer, J., Munro, C.S., Jonkman, M.F., van Steensel, M.A.M., van Geel, M.

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Molecular genetic support for the rule of dichotomy in type 2 segmental Darier disease: Correspondence von Fölster-Holst, R., Nellen, R.G.L., Jensen, J.-M., Poblete-Gutiérrez, P., Steijlen, P.M., Schwarz, T., Happle, R., Van Geel, M., Frank, J.

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